Pharmacokinetics Flashcards

1
Q

What is bioavailability?

A

The fraction of a drug that reaches the systemic circulation after oral dosing

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2
Q

Name three ways drugs get transported around the body

A

Protein binding
Blood flow
Lipid solubility

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3
Q

Where are drugs metabolised and excreted?

A

Metabolised in liver

Excreted in kidneys

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4
Q

What happens to lipid soluble drugs in the liver?

A

Converted to water soluble so can be excreted by adding a conjugate or modifying the drugs structure

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5
Q

Metabolism can deactivate or activate drugs. Explain

A

When a drug is metabolised to water soluble it’s effect and toxicity reduce.
But some drugs are coated and only becomes activated when metabolised by the liver.

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6
Q

What is a prodrug?

A

Only activated when it reaches the liver

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7
Q

Where are antivirals activated?

A

Their site of action

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8
Q

Drugs can affect the liver and it’s metabolism, name two ways

A

Inhibitors or inducers

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9
Q

What happens if you take an inhibitor drug along with a substrate ?

A

The substrate will have a heightened effect as the liver metabolism enzymes have been inhibited by the inhibitor drug

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10
Q

What is genetic polymorphism?

A

Some people do not have the enzymes to metabolise drugs so they have no effect

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11
Q

What types of drugs are filtered by glomerular filtration?

A

Unbound

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12
Q

How are free and bound drugs secreted?

A

Active secretion

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13
Q

What is passive reabsorption?

A

Drug is transferred back to blood usually from the intestines if it has been excreted by the liver into bile

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14
Q

In an overdose case, how would you make the excretion of a drug quicker?

A

Make the urine acidic

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15
Q

What is the renal clearance equation?

A

Rate of excretion / plasma concentration

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